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Competence-Stimulating Peptide-12261
CAS No. 1235882-91-3
Competence-Stimulating Peptide-12261( —— )
Catalog No. M30330 CAS No. 1235882-91-3
Competence-Stimulating Peptide-12261, a sixteen peptide, is a fragment of competence-stimulating peptide.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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Biological Information
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Product NameCompetence-Stimulating Peptide-12261
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NoteResearch use only, not for human use.
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Brief DescriptionCompetence-Stimulating Peptide-12261, a sixteen peptide, is a fragment of competence-stimulating peptide.
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DescriptionCompetence-Stimulating Peptide-12261, a sixteen peptide, is a fragment of competence-stimulating peptide.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1235882-91-3
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Formula Weight2153.45
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Molecular FormulaC100H149N31O23
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical NameSequence:{Glu}{Ile}{Arg}{Gln}{Thr}{His}{Asn}{Ile}{Phe}{Phe}{Asn}{Phe}{Phe}{Lys}{Arg}{Arg}
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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[Leu144,Arg147]-Myel...
[Leu144,Arg147]-PLP (139-151) is a mutant peptide fragment of myelin proteolipid protein (PLP), with the tryptophan and histidine at positions 144 and 147 respectively replaced by leucine and arginine. [Leu144,Arg147]-PLP (139-151) also serves as a T cell receptor (TCR) antagonist for encephalitogenic Th1 clones, blocking their activation in vitro. Furthermore, [Leu144,Arg147]-PLP (139-151) can inhibit the development of experimental autoimmune encephalomyelitis (EAE).
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1-((3R,4S)-3-hydroxy-2,2-dimethyl-6-(phenylsulfonyl)chroman-4-yl)pyrrolidin-2-one is an isomer of Rilmakalim, a potassium channel opener (PCO), which can activate ATP-sensitive K+ channels in the heart or other tissues
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SLF-amido-C2-COOH
SLF-amido-C2-COOH (ZZY01-083) is an FKBP ligand with potential antimicrobial activity for the synthesis of PROTAC.
